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我父亲肺鳞癌的治疗贴(2014年3月1日驾鹤西去)

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1118553 1620 老马 发表于 2011-10-27 08:05:18 | 置顶 |
老马  博士一年级 发表于 2012-4-27 18:50:42 | 显示全部楼层 来自: 浙江温州
Pooled Analysis of S-1 Trials in Non-Small Cell Lung Cancer According to Histological Type
) t+ w& d$ ~- b1 TNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 ! ]8 u2 U2 ]7 e) e% A3 p
+ Author Affiliations
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1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
, z% N( E4 T- d& e+ U4 G2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
) ~7 E! N& C% H' z( @* s9 A) R3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan ) T% S+ h" R+ v" p
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan # I0 @$ Q: L# x- Z. P3 H/ q! M( ?
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
2 f) g* O: y! V" L" V+ S7 P, {6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
  A9 V4 g+ R: P: T7Kinki University School of Medicine, Osaka 589-8511, Japan 8 E, d' m7 \5 P& o) O8 d
8Izumi Municipal Hospital, Osaka 594-0071, Japan
9 f& o, S4 ^$ \6 l+ k9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
, w4 ^3 M$ f# [4 d6 ]! n( BCorrespondence to: Nobuyuki Yamamoto, Division of Thoracic Oncology, Shizuoka Cancer Center, 1007 Shimonagakubo, Nagaizumi-cho, Sunto-gun, Shizuoka 411-8777, Japan. Tel: +81 559895222, Fax: +81 559895783, e-mail: n.yamamoto@scchr.jp 9 V$ d/ y- ]$ F8 w
AbstractBackground: The antimetabolic agent S-1 inhibits thymidylate synthase similar to pemetrexed, but through a different mechanism of action. Whether the antitumour activity of S-1 depends on histological type remains unclear. We analysed pooled data from 2 phase II clinical studies of cisplatin and S-1 in patients with previously untreated advanced non-small cell lung cancer. Patients and Methods: We comprised 110 patients with stage IIIB or IV non–small cell lung cancer. Univariate and multivariate analyses were performed to determine the effects of histological type on progression-free survival and response rates. Results: On pooled analysis of the data, according to histological type, median progression-free survival was 3.8 months in patients with squamous cell carcinoma and 4.4 months in those with non-squamous cell carcinoma. Both analyses showed that progression-free survival and response rate did not differ significantly. Conclusion: Unlike molecular targeted agents and pemetrexed, a combination of cisplatin and S-1 may be no difference in response according to histological type.
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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:52:43 | 显示全部楼层 来自: 浙江温州
S-1 monotherapy for previously treated non-small cell lung cancer: A retrospective analysis by age and histopathological type
5 c3 I, r0 x! F7 T' {' G
' E2 I$ \" ^4 q$ p7 r" XAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato . g, v+ O7 d2 q- M" ~
3 r$ t& I" b/ G6 l+ p7 q
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
2 I" ^7 Z9 K9 ^& Z# Q8 b
, Y+ K5 H( t/ P3 Z! T; c) u7 B# V$ tPublished online on: Thursday, December 1, 2011
& |& y3 O- {3 C7 J' c! K# R1 B! X/ F1 }9 E- J: F) e( a2 ~6 A3 `
Doi: 10.3892/ol.2011.507
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- L( Q* J5 k4 nPages: 405-410
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Abstract:
  ?0 \9 a0 f% aS-1, an oral fluoropyrimidine derivative, has been approved for the treatment of non-small cell lung cancer (NSCLC) in Japan. In the present study, the efficacy and safety of S-1 monotherapy for elderly patients with previously treated NSCLC were retrospectively evaluated, and the efficacy of S-1 monotherapy was compared by histopathological type. This retrospective study included 54 patients with advanced or recurrent NSCLC who had received S-1 monotherapy following the failure of previous chemotherapy regimens at our institutes. Patient outcomes were compared based on their age and histopathological type. S-1 was administered orally, twice daily, while the duration and interval were modified according to the medical condition of each patient. The default delivery schedule, the mean number of S-1 cycles, did not differ significantly between the two age groups (<70 and ≥70 years). The rate of therapy discontinuation, schedule modification or dose reduction due to intolerable toxicities or patient refusal was relatively frequent in the older group (40.7 and 55.6% for ages <70 and ≥70 years, respectively; p=0.414), and the incidence of grade 3 anemia was relatively high in the older group (3.7 and 18.5%, respectively; p=0.192). The response rates (13.0 and 4.8%, respectively; p=0.609) and disease control rates (39.1 and 33.3%, respectively; p=0.761) did not differ significantly between the two age groups. According to histopathological type, the disease control rate was significantly higher in adenocarcinoma (57.9%) compared to non-adenocarcinoma (20.0%, p=0.013). Thus, S-1 monotherapy may be equally effective and tolerated in patients <70 years and those ≥70 years. Additionally, adenocarcinoma may have a higher disease control rate than non-adenocarcinoma.
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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:57:27 | 显示全部楼层 来自: 浙江温州
Thymidylate synthase (TS) gene expression in primary lung cancer patients: a large-scale study in Japanese population1 b3 U' W3 \" U7 z
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
9 `9 U9 F8 O6 `% X: r, i8 v+ Author Affiliations7 @5 ?. U/ r9 M0 J# G( T, V
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
7 H& V+ _! `1 y; T2Department of Thoracic Surgery, Kyoto University, Kyoto
+ h2 a+ z. s3 b7 C/ b3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan ' G( Q* ?" A8 b/ i
&#8629;*Correspondence to: Dr F. Tanaka, Second Department of Surgery, University of Environmental and Occupational Health, 1-1 Isegaoka, Yahata-nishi, Kitakakyushu, 807-8555, Japan. Tel: +81-93-891-7442; Fax: +81-93-692-4004; E-mail: ftanaka@med.uoeh-u.ac.jp 9 q5 h( z6 ]6 r7 e
Received September 3, 2010. + Y) V( E  ?. ^* P
Revision received November 11, 2010.
( V9 F- s' U$ o$ L' O7 `% hAccepted November 17, 2010. 2 g5 h! m6 O. x/ @3 A; q$ i
Abstract  a( r2 X: R7 D# A
Background: Previous small-sized studies showed lower thymidylate synthase (TS) expression in adenocarcinoma of the lung, which may explain higher antitumor activity of TS-inhibiting agents such as pemetrexed. " Y5 {0 V% t( h0 O
Patients and methods: To quantitatively measure TS gene expression in a large-scale Japanese population (n = 2621) with primary lung cancer, laser-captured microdissected sections were cut from primary tumors, surrounding normal lung tissues and involved nodes.
8 F$ H7 m6 U- F& g+ @, c: C0 h. zResults: TS gene expression level in primary tumor was significantly higher than that in normal lung tissue (mean TS/β-actin, 3.4 and 1.0, respectively; P < 0.01), and TS gene expression level was further higher in involved node (mean TS/β-actin, 7.7; P < 0.01). Analyses of TS gene expression levels in primary tumor according to histologic cell type revealed that small-cell carcinoma showed highest TS expression (mean TS/β-actin, 13.8) and that squamous cell carcinoma showed higher TS expression as compared with adenocarcinoma (mean TS/β-actin, 4.3 and 2.3, respectively; P < 0.01); TS gene expression was significantly increased along with a decrease in the grade of tumor cell differentiation. There was no significant difference in TS gene expression according to any other patient characteristics including tumor progression. % M6 A! c3 X  J0 t. Q' T4 A
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. 7 O. A, p. h- ?/ r% D9 j3 e' A) M
个人公众号:treeofhope
走在异乡  高中一年级 发表于 2012-4-28 00:30:22 | 显示全部楼层 来自: 四川成都
一直关注老马的帖子,前方的指明灯。祝福你爸好疗效
累计签到:1 天
连续签到:1 天
[LV.1]初来乍到
baiselianyi  初中二年级 发表于 2012-4-28 10:24:44 | 显示全部楼层 来自: 浙江台州
一直得到老马帮助,祝福老马爸爸
老马  博士一年级 发表于 2012-4-28 18:00:37 | 显示全部楼层 来自: 浙江温州
26日吃了12片地米(0.75mg一片),27日吃了22片地米(0.75mg 一片),28日吃了12片地米(0.75mg一片),都分二次吃。8 ?9 m5 p( U9 s0 `% |0 _
今天为止没有任何反应,每天吃VC,VB2,还有漱口水,就怕口腔溃疡。
个人公众号:treeofhope
bishop_cn  大学一年级 发表于 2012-4-28 23:16:11 | 显示全部楼层 来自: 中国
副作用如何,单药反应很小吧?; H8 n: ?: }! G" w( P( V
老马  博士一年级 发表于 2012-4-29 00:20:00 | 显示全部楼层 来自: 浙江温州
LUX-Lung 8: A Phase III Trial of Afatinib (BIBW 2992) Versus Erlotinib for the Treatment of Squamous Cell Lung Cancer After at Least One Prior Platinum Based Chemotherapy" I+ m/ Y7 @3 g: j6 H" \* w
http://clinicaltrials.gov/ct2/show/NCT015235875 f% o* e9 I4 A, F# x. J1 i3 B; F

4 ]! H- z4 U" q$ m4 ^. T% WBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC% Z& M* e5 E5 B; w. u% P
http://clinicaltrials.gov/ct2/show/NCT01156545
个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-29 20:53:58 | 显示全部楼层 来自: 浙江温州
本帖最后由 老马 于 2012-4-30 09:33 编辑 4 U# Z5 }; F! z( }) {4 B
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从4月24日开始到4月28日,打了5天的舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。
# j, C: f: f0 ]1 k8 l. U至今为止,未出现化疗副作用。
个人公众号:treeofhope
英雄武松  大学四年级 发表于 2012-4-30 01:37:05 | 显示全部楼层 来自: 哈萨克斯坦

0 o& Q7 Z7 f) `2 O+ }没有副作用是第一追求,效果显著是第二追求。
, }# h- n# ^& f* u不错。

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